3-Methyl-3-buten-1-OL

Details

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Internal ID 797482ac-7551-402e-bda9-082677db7df9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 3-methylbut-3-en-1-ol
SMILES (Canonical) CC(=C)CCO
SMILES (Isomeric) CC(=C)CCO
InChI InChI=1S/C5H10O/c1-5(2)3-4-6/h6H,1,3-4H2,2H3
InChI Key CPJRRXSHAYUTGL-UHFFFAOYSA-N
Popularity 198 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O
Molecular Weight 86.13 g/mol
Exact Mass 86.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3-Methylbut-3-en-1-ol
763-32-6
Isoprenol
3-Buten-1-ol, 3-methyl-
Isobutenylcarbinol
Methallylcarbinol
2-Methyl-1-buten-4-ol
3-Isopentenyl alcohol
Isopropenylethyl alcohol
3-methyl-3-butenol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Methyl-3-buten-1-OL

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.7989 79.89%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.6935 69.35%
OATP2B1 inhibitior - 0.8663 86.63%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9403 94.03%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9750 97.50%
CYP3A4 substrate - 0.7586 75.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8986 89.86%
CYP2C9 inhibition - 0.9408 94.08%
CYP2C19 inhibition - 0.8850 88.50%
CYP2D6 inhibition - 0.9338 93.38%
CYP1A2 inhibition - 0.7401 74.01%
CYP2C8 inhibition - 0.9870 98.70%
CYP inhibitory promiscuity - 0.8897 88.97%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6952 69.52%
Eye corrosion + 0.8522 85.22%
Eye irritation + 0.9908 99.08%
Skin irritation + 0.8080 80.80%
Skin corrosion - 0.7142 71.42%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7274 72.74%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5235 52.35%
skin sensitisation + 0.7317 73.17%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7305 73.05%
Acute Oral Toxicity (c) III 0.7870 78.70%
Estrogen receptor binding - 0.9444 94.44%
Androgen receptor binding - 0.9393 93.93%
Thyroid receptor binding - 0.8993 89.93%
Glucocorticoid receptor binding - 0.9274 92.74%
Aromatase binding - 0.8900 89.00%
PPAR gamma - 0.9307 93.07%
Honey bee toxicity - 0.9273 92.73%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.5000 50.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.00% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.15% 83.82%
CHEMBL2581 P07339 Cathepsin D 84.54% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Artemisia argyi
Artemisia montana
Artemisia princeps
Cananga odorata
Citrus × aurantium
Croton eluteria
Dactylanthus taylorii
Pandanus tectorius
Persicaria bistorta
Quercus ilex
Vitis vinifera

Cross-Links

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PubChem 12988
NPASS NPC28077
LOTUS LTS0197023
wikiData Q408094